NP-MRD: Showing NP-Card for (3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione (NP0215512)

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Record Information

Version

2.0

Created at

2022-09-05 15:09:27 UTC

Updated at

2022-09-05 15:09:27 UTC

NP-MRD ID

NP0215512

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione

Description

Aspochalasin P belongs to the class of organic compounds known as aspochalasins. These are cytochalasans with a structure in which the hydrogenated isoindole bears a 2-methylpropyl group. (3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione is found in Mariannaea elegans. Based on a literature review very few articles have been published on Aspochalasin P.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052217092D          

 29 31  0  0  1  0            999 V2000
   -0.5979   -1.0236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0621   -1.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8256   -1.2450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4780   -1.7500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2979   -1.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6562   -0.6289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3437    0.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737   -0.7401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6206   -1.5519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3098   -2.1349    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1077   -1.8118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1987   -2.9524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8982   -3.4602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4352   -3.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7828   -2.7600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0644   -2.9649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1002   -4.0043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3669   -2.5675    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9000   -3.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6761   -3.5957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4660   -3.8987    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6646   -3.7027    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0425   -4.3056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0408   -5.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7544   -5.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6745   -5.5596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6033   -2.8800    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0491   -2.3750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8919   -2.6297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 27 22  1  6  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END

     RDKit          3D

 64 66  0  0  0  0  0  0  0  0999 V2000
    1.5782   -3.7099   -2.0154 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9458   -2.7170   -1.1132 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2233   -2.1907   -1.4417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7976   -1.1810   -0.4494 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2234   -1.0729   -0.5523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2038   -0.2263   -0.6310 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6686   -0.7508   -0.7299 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2289    1.2558   -0.6506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2901    1.8762    0.1949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0468    1.9891    1.6346 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2087    1.9071    2.4228 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0556    1.0554    2.2087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4135   -0.1083    2.3101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7053    1.3993    2.6586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6764    0.3724    2.1598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1196    0.7949    0.8636 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1256    1.9761    0.7255 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1666   -0.1092   -0.2926 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5252    0.6980   -1.4420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2685    1.6059   -2.1262 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7200    0.5404   -1.8591 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4546   -0.4232   -1.0807 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8250    0.0333   -0.9293 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1662    1.3016   -0.2722 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7640    1.4439    1.1677 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7460    2.5380   -1.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5646   -0.6987    0.0580 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4997   -2.2309    0.1680 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9542   -2.7116    0.2939 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7559   -4.4427   -2.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3518   -4.3165   -1.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8809   -3.2898   -2.9969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7673   -2.4299   -2.3382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6416   -1.7592    0.5472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6998   -2.1331   -0.5794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1362   -0.7428    0.2495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2441   -0.1804   -1.4400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6303   -1.8035   -1.0805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3173    1.7840   -0.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4663    1.5299   -1.7313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5520    2.8819   -0.2016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2325    1.2770    0.0568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6477    3.0088    1.8352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5345    0.9760    2.5075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7128    1.4123    3.7802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4388    2.4130    2.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0847   -0.6432    2.1883 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1701    0.3883    2.8935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4718    2.5379   -1.8033 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5041   -1.3160   -1.7947 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5495   -0.7376   -0.5157 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2279    0.1219   -1.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3000    1.3625   -0.2624 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9850    0.5024    1.7508 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7489    1.8335    1.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4239    2.1984    1.7033 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6883    2.7889   -0.9196 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9775    2.4544   -2.1083 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3403    3.3905   -0.6336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8995   -0.3848    1.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0412   -2.5948    1.0767 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9101   -3.7698    0.7031 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4327   -2.8193   -0.6731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4850   -2.1549    1.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24 26  1  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 19  2  0
 19 20  1  0
 18 19  1  6
 18 27  1  0
 27 28  1  0
 28 29  1  0
 28  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 27 22  1  0
  4 18  1  0
 16 18  1  0
 25 54  1  0
 25 55  1  0
 25 56  1  0
 24 53  1  0
 26 57  1  0
 26 58  1  0
 26 59  1  0
 23 51  1  0
 23 52  1  0
 22 50  1  6
 20 49  1  0
 27 60  1  1
 28 61  1  1
 29 62  1  0
 29 63  1  0
 29 64  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  3 33  1  0
  4 34  1  1
  5 35  1  0
  7 36  1  0
  7 37  1  0
  7 38  1  0
  8 39  1  0
  8 40  1  0
  9 41  1  0
  9 42  1  0
 10 43  1  6
 11 44  1  0
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
M  END


  Mrv1652309052217092D          

 29 31  0  0  1  0            999 V2000
   -0.5979   -1.0236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0621   -1.5575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8256   -1.2450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4780   -1.7500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2979   -1.3721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6562   -0.6289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3437    0.1661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4737   -0.7401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6206   -1.5519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3098   -2.1349    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1077   -1.8118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1987   -2.9524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8982   -3.4602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4352   -3.2649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7828   -2.7600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0644   -2.9649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1002   -4.0043    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3669   -2.5675    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9000   -3.1971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6761   -3.5957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4660   -3.8987    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6646   -3.7027    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0425   -4.3056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0408   -5.1486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7544   -5.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6745   -5.5596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6033   -2.8800    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0491   -2.3750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8919   -2.6297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  4  3  1  6  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
  4 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 27 22  1  6  0  0  0
 18 27  1  0  0  0  0
 27 28  1  0  0  0  0
  2 28  1  0  0  0  0
 28 29  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0215512

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C[C@@H]1N=C(O)[C@]23[C@H]1[C@H](C)C(C)=C[C@@H]2\C=C(C)\CC[C@@H](O)C(=O)CCC3=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H35NO4/c1-13(2)10-18-22-16(5)15(4)12-17-11-14(3)6-7-19(26)20(27)8-9-21(28)24(17,22)23(29)25-18/h11-13,16-19,22,26H,6-10H2,1-5H3,(H,25,29)/b14-11+/t16-,17+,18+,19-,22+,24-/m1/s1

> <INCHI_KEY>
ULCFKAWMNZMXPT-RRRFKTONSA-N

> <FORMULA>
C24H35NO4

> <MOLECULAR_WEIGHT>
401.547

> <EXACT_MASS>
401.256608611

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
45.35794705348102

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4S,6aS,11R,15aR,15bR)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3H,4H,6aH,9H,10H,11H,12H,13H,14H,15H,15bH-cycloundeca[e]isoindole-12,15-dione

> <JCHEM_LOGP>
2.810299368600589

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.389706687997268

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8873588675728863

> <JCHEM_PKA_STRONGEST_BASIC>
5.64286504430879

> <JCHEM_POLAR_SURFACE_AREA>
86.96000000000001

> <JCHEM_REFRACTIVITY>
114.94489999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4S,6aS,11R,15aR,15bR)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3H,4H,6aH,9H,10H,11H,13H,14H,15bH-cycloundeca[e]isoindole-12,15-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.116  -1.911   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.116  -2.907   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.541  -2.324   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.759  -3.267   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.289  -2.561   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.958  -1.174   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.375   0.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.484  -1.381   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.758  -2.897   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.045  -3.985   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       9.534  -3.382   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.838  -5.511   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.143  -6.459   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       6.412  -6.095   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.195  -5.152   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.853  -5.534   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.920  -7.475   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.551  -4.793   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.547  -5.968   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.995  -6.712   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0       2.737  -7.278   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       1.241  -6.912   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.079  -8.037   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.076  -9.611   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.408 -10.383   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.259 -10.378   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.126  -5.376   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.092  -4.433   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.665  -4.909   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   18                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16    4   19   27                                             
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   22   18   28                                                  
CONECT   28   27    2   29                                                  
CONECT   29   28                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₅NO₄

Average Mass

401.5470 Da

Monoisotopic Mass

401.25661 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C[C@@H]1N=C(O)[C@]23[C@H]1[C@H](C)C(C)=C[C@@H]2\C=C(C)\CC[C@@H](O)C(=O)CCC3=O

InChI Identifier

InChI=1S/C24H35NO4/c1-13(2)10-18-22-16(5)15(4)12-17-11-14(3)6-7-19(26)20(27)8-9-21(28)24(17,22)23(29)25-18/h11-13,16-19,22,26H,6-10H2,1-5H3,(H,25,29)/b14-11+/t16-,17+,18+,19-,22+,24-/m1/s1

InChI Key

ULCFKAWMNZMXPT-RRRFKTONSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Mariannaea elegans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aspochalasins. These are cytochalasans with a structure in which the hydrogenated isoindole bears a 2-methylpropyl group.

Kingdom

Organic compounds

Super Class

Alkaloids and derivatives

Class

Cytochalasans

Sub Class

Aspochalasins

Direct Parent

Aspochalasins

Alternative Parents

Substituents

Aspochalasin skeleton
Carbocyclic aspochalasin skeleton
Isoindolone
Isoindoline
Isoindole
Isoindole or derivatives
Pyrrolidone
2-pyrrolidone
Pyrrolidine
Secondary carboxylic acid amide
Secondary alcohol
Cyclic ketone
Carboxamide group
Lactam
Ketone
Organoheterocyclic compound
Azacycle
Carboxylic acid derivative
Alcohol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

27024269

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44471449

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione (NP0215512)

MOL for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D MOL for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D SDF for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D-SDF for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

PDB for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D PDB for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

SMILES for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

INCHI for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

Structure for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)

3D Structure for NP0215512 ((3s,3ar,4s,6as,11r,15ar)-1,11-dihydroxy-4,5,8-trimethyl-3-(2-methylpropyl)-3h,3ah,4h,6ah,9h,10h,11h,13h,14h-cycloundeca[d]isoindole-12,15-dione)